Reverse shoulder arthroplasty (RSA) is commonly used to treat patients with rotator cuff tear arthropathy. Loosening of the glenoid component remains one of the principal modes of failure and is the main complication leading to revision. For optimal RSA implant osseointegration to occur, the micromotion between the baseplate and the bone must not exceed a threshold of 150 µm. Excess micromotion contributes to glenoid loosening. This study assessed the effects of various factors on glenoid baseplate micromotion for primary fixation of RSA. A half-fractional factorial experiment design (2k-1) was used to assess four factors: central element type (central peg or screw), central element cortical engagement according to length (13.5 or 23.5 mm), anterior-posterior (A-P) peripheral screw type (nonlocking or locking), and bone surrogate density (10 or 25 pounds per cubic foot [pcf]). This created eight unique conditions, each repeated five times for 40 total runs. Glenoid baseplates were implanted into high- or low-density Sawbones™ rigid polyurethane (PU) foam blocks and cyclically loaded at 60 degrees for 1000 cycles (500 N compressive force range) using a custom designed loading apparatus. Micromotion at the four peripheral screw positions was recorded using linear variable displacement transducers (LVDTs). Maximum micromotion was quantified as the displacement range at the implant-PU interface, averaged over the last 10 cycles of loading. Baseplates with short central elements that lacked cortical bone engagement generated 373% greater maximum micromotion at all peripheral screw positions compared to those with long central elements (p < 0.001). Central peg fixation generated 360% greater maximum micromotion than central screw fixation (p < 0.001). No significant effects were observed when varying A-P peripheral screw type or bone surrogate density. There were significant interactions between central element length and type (p < 0.001). An interaction existed between central element type and level of cortical engagement. A central screw and a long central element that engaged cortical bone reduced RSA baseplate micromotion. These findings serve to inform surgical decision-making regarding baseplate fixation elements to minimize the risk of glenoid loosening and thus, the need for revision surgery.
The purpose of this study is to quantify the distribution of bone density in the scapulae of patients undergoing reverse shoulder arthroplasty (RSA) to guide optimal screw placement. To achieve this aim, we compared bone density in regions around the glenoid that are targeted for screw placement, as well as bone density variations medial to lateral within the glenoid. Specimen included twelve scapula in 12 patients with a mean age of 74 years (standard deviation = 9.2 years). Each scapula underwent a computed tomography (CT) scan with a Lightspeed+ XCR 16-Slice CT scanner (General Electric, Milwaukee, USA). Three-dimensional (three-D) surface mesh models and masks of the scapulae containing three-D voxel locations along with the relative Hounsfield Units (HU) were created. Regions of interest (ROI) were selected based on their potential glenoid baseplate screw positioning in RSA surgery. These included the base of coracoid inferior and lateral to the suprascapular notch, an anterior and posterior portion of the scapular spine, and an anterosuperior and inferior portion of the lateral border. Five additional regions resembling a clock face, on the glenoid articular surface were then selected to analyze medial to lateral variations in bone density including twelve, three, six, and nine-o'clock positions as well as a central region. Analysis of Variance (ANOVA) tests were used to examine statistical differences in bone density between each region of interest (p < 0 .05). For the regional evaluation, the coracoid lateral to the suprascapular notch was significantly less dense than the inferior portion of the lateral border (mean difference = 85.6 HU, p=0.03), anterosuperior portion of the lateral border (mean difference = 82.7 HU, p=0.04), posterior spine (mean difference = 97.6 HU, p=0.007), and anterior spine (mean difference = 99.3 HU, p=0.006). For the medial to lateral evaluation, preliminary findings indicate a “U” pattern with the densest regions of bone in the glenoid most medially and most laterally with a region of less dense bone in-between. The results from this study utilizing clinical patient CT scans, showed similar results to those found in our previous cadaveric study where the coracoid region was significantly less dense than regions around the lateral scapular border and scapular spine. We also have found for medial to lateral bone density, a “U” distribution with the densest regions of bone most medially and most laterally in the glenoid, with a region of less dense bone between most medial and most lateral. Clinical applications for our results include a carefully planned trajectory when placing screws in the scapula, potentially avoiding the base of coracoid. Additionally, surgeons may choose variable screw lengths depending on the region of bone and its variation of density medial to lateral, and that screws that pass beyond the most lateral (subchondral) bone, will only achieve further purchase if they enter the denser bone more medially. We suspect that if surgeons strategically aim screw placement for the regions of higher bone density, they may be able to decrease micromotion in baseplate fixation and increase the longevity of RSA.
Reverse shoulder arthroplasty (RSA) has an increasing effective use in the treatment of patients with a variety of diagnoses, including rotator cuff deficiency, inflammatory arthritis, or failed shoulder prostheses. Glenoid bone loss is not uncommonly encountered in these cases due to the significant wear. Severe bone loss can compromise glenoid baseplate positioning and fixation, consequently increasing the risk for early component loosening, instability, and scapular notching. To manage severe glenoid bone deficiencies, bone grafts are commonly used. Although, many studies report outcome of bone grafting in revision RSA, the literature on humeral head autograft for glenoid bone loss in primary RSA is less robust. The purpose of this study is to evaluate the clinical and radiographic outcomes of primary RSA with humeral head autograft for glenoid bone loss at our institution. Institutional review board approval was obtained to retrospectively review the records of 22 consecutive primary RTSA surgeries in 21 patients with humeral head autograft for glenoid bone loss between January 2008 and December 2016. Five patients died during follow-up, three were unable to be contacted and one refused to participate, leaving a final study cohort of 12 patients with 13 shoulders that underwent RSA. All patients had a clinical evaluation including detailed ROM and clinical evaluation using the American Shoulder and Elbow Surgeons (ASES) Score, Constant Score, Western Ontario Osteoarthritis of the Shoulder Index (WOOS), and Short Form-12 (SF-12) questionnaires. Preoperative and postoperative plain radiographs and CT scans were assessed for component position, loosening, scapular notching, as well as graft incorporation, resorption, or collapse. There were 6 males and 6 females, with an average age of 74 ± 6.8 years. The average BMI was 31.7 ± 5.3, and the median ASA score was 3. Average follow-up was 3.4 ± 1.1 years. The average postoperative range of motion measurements for the operative arm are: flexion = 120 ± 37, abduction = 106 ± 23, external rotation = 14 ± 12, internal rotation at 90 degrees of abduction = 49 ± 7, external rotation at 90 degrees of abduction = 50 ± 28. Average functional scores are: ASES: 76.9 ± 19.2, WOOS: 456 ± 347, SF12 physical: 34.2 ± 8.2, SF12 mental: 54.1 ± 10.2, Constant Score: 64.6 ± 14. No evidence of hardware loosening or evidence of bone graft resorption were encountered. On CT, the average of pre operative B-angle was 79.3 ± 9.3 while the pre operative reverse shoulder angle was 101.4 ± 28. Glenoid retroversion average on CT was 13.3 ± 16.6. Post operative baseplate inclination average was 82 ± 7.4 while the baseplate version 7.8 ±10. The operative technique was able to achieve up to 30 degrees of inclination correction and up to 50 degrees of version correction. In conclusion, primary reverse shoulder arthroplasty with humeral head autograft for glenoid bone loss provides excellent ROM and functional outcomes at mid-term follow-up. This technique has a high rate of bone incorporation and small risk of bone resorption at mid term follow up.
While reverse shoulder arthroplasty (RSA) is a reliable treatment option for patients with rotator cuff deficiency, loss of glenoid baseplate fixation often occurs due to screw loosening. We questioned whether an analysis of the trabecular bone density distribution in the scapula would indicate more optimal sites for screw placement. As such, the purpose of this study was to determine the anatomic distribution of trabecular bone density in regions of the scapula available for screw placement in RSA. Seven cadaveric shoulders were computed tomography (CT) scanned, and then voxels of the scapulae were isolated from the CT volume (Mimics 15.0 Materialise, Leuven, Belgium). Analyses were conducted in a common, 3D coordinate system. Volumetric regions of interest (ROI) within the scapula were identified based on potential baseplate screw sites. ROIs included areas at the base of the coracoid process lateral and inferior to the suprascapular notch, in the posterior and anterior lateral spine and in the anterosuperior and posteroinferior lateral border. Hounsfield Units (HU) were extracted from voxels corresponding to trabecular bone within each ROI. Overall bone density was summarised as the frequency of HU values above 80% of the ROI's maximum density value. Paired, two-tailed t-tests assuming unequal variance were used for pairwise comparisons (P≤0.05). Intra-region analyses compared two ROIs within the same broad anatomical structure; inter-region analyses compared ROIs between anatomical structures. Areas of the spine and lateral border of the scapula appeared to be denser than the coracoid process. Intra-region comparisons indicated no significant differences within ROI: coracoid P=0.43, spine P=0.95, lateral border P=0.41. ROI inferior to the suprascapular notch were on average 3.78% (P=0.08) and 6% (P=0.04) less dense than the anterosuperior and posteroinferior lateral border and 7.59% (P=0.006) and 7.72% (P=0.01) less dense than the anterior and posterior lateral spine. ROI lateral to the suprascapular notch were 6% (P=0.05) and 8.21% (P=0.02) less dense than the anterosuperior and posteroinferior lateral border and 9.8% (P=0.006) and 9.94% (P=0.008) less dense than the anterior and posterior lateral spine. There was no significant difference between the anterior spine and anterosuperior and posteroinferior lateral border (P=0.12, P=0.58), nor between the posterior spine and anterosuperior and posteroinferior lateral border (P=0.14, P=0.57). Results from this study indicate that the spine and lateral border of the scapula contain denser trabecular bone relative to regions in the coracoid. The higher quality bone of the spine and lateral border should be favoured over the coracoid process when fixing the glenoid baseplate in RSA. Further research may support the redesign of the glenoid baseplate geometry to better integrate the anatomy of the scapula and improve implant survival.
Estimated to affect 2–5% of the population, adhesive capsulitis is a common cause of shoulder pain and dysfunction. The objective of this study is to determine if arthrographic injection of the shoulder joint with steroid, local anesthetic and contrast is an effective treatment modality for adhesive capsulitis and whether it is superior to arthrographic injection with local anesthetic and contrast alone. This is a double-blinded RCT of patients with a diagnosis of adhesive capsulitis who were randomly assigned to receive an image guided arthrographic glenohumeral injection with either triamcinalone (steroid), lidocaine (local anesthetic) and contrast or lidocaine and contrast alone. Outcome measures included active and passive shoulder range of motion (ROM) and functional outcomes assessed using the Shoulder Pain and Disability Index (SPADI), the Constant Score and a Visual Analog Scale for pain. Post-operative evaluation occurred at 3 weeks, 6 weeks and 12 weeks. Descriptive statistics were utilised to summarise patient demographics and other study parameters. One-way ANOVAs compared the VAS, Constant and SPADI scores across the different time points for both study groups. The post hoc Bonferroni correction was used to adjust for multiple comparisons. There were 37 shoulders injected with follow-up visits at 12 weeks. Twenty shoulders were randomised to receive local plus steroid and 17 shoulders received local anesthetic only. There were 21 females and 14 males with an average age of 54 years (range, 42–70). VAS scores for both patient groups were significantly improved (p<0.05) at all follow-up times. Goniometric testing demonstrated significant improvements in forward flexion and internal rotation at 90 degrees in the local group and only abduction in the local plus steroid group. There were no significant changes in the Constant scores for the local group (p=0.08), however, the Constant scores showed significant improvement for the local plus steroid group (p=0.003) at all follow-up time points. The local group showed significant improvement in their SPADI pain scores at the 12 week follow-up only (p=0.01). There were no significant differences in their SPADI disability scores (p=0.09). The local plus steroid group had significant improvement in SPADI pain and disability scores at all follow-up time points (p=0.001). The optimal treatment for adhesive capsulitis remains unclear. Our study demonstrated that patients receiving an arthrographic injection of either steroid and local anesthetic or local anesthetic alone had significantly improved post-injection pain scores. However, only the steroid and local anesthetic group demonstrated improved SPADI disability and Constant scores. Thus, we believe that either treatment may be a good option for patients with adhesive capsulitis and can reliably relieve pain, but we would recommend the steroid with local anesthetic over the local anesthetic alone as it may provide improved function.
Reverse shoulder arthroplasty has a high complication rate related to glenoid implant instability and screw loosening. Better radiographic post-operative evaluation may help in understanding complications causes. Medical radiographic imaging is the conventional technique for post-operative component placement analysis. Studies suggest that volumetric CT is better than use of CT slices or conventional radiographs. Currently, post-operative CT use is limited by metal-artifacts in images. This study evaluated inter-observer reliability of pre-operative and post-operative CT images registration to conventional approaches using radiographs and CT slices in measuring reverse shoulder arthroplasty glenoid implant and screw percentage in bone. Pre-operative and post-operative CT scans, and post-operative radiographs were obtained from six patients that had reverse shoulder arthroplasty. CT scans images were imported into a medical imaging processing software and each scapula, glenoid implant and inferior screw were reconstructed as 3D models. Post-operative 3D models were imported into the pre-operative reference frame and matched to the pre-operative scapula model using a paired-point and a surface registration. Measurements on registered CT models were done in reference to the pre-operative scapula model coordinate frame defined by a computer-assisted designed triad positioned in respect to the center of the glenoid fossa and trigonum scapulae (medial-lateral, z axis) and superior and inferior glenoid tubercle (superior-inferior, y axis). The orthogonal triad third axis defined the anterior-posterior axis (x axis). A duplicate triad was positioned along the central axis of the glenoid implant model. Using a virtual protractor, the glenoid implant inclination was measured from its central axis and the scapula transverse plane (x - z axes) and version from the coronal plane (y - z axes). Inferior screw percentage in bone was measured from a Boolean intersection operation between the pre-operative scapula model and the inferior screw model. For CT slices and radiographic measurements, a first 90-degree Cobb angle, from medical records software, was positioned from the trigonum scapulae to the centre of the central peg. Using the 90-degree line as reference, a second Cobb angle was drawn from the most superior to the most inferior point of the glenoid implant for inclination and from of the most anterior to the most posterior point for version. Version can only be measured using CT slices. Screw percentage in bone was calculated from screw length measures collected with a distance-measuring tool from the software. For testing the inter-observer reliability of the three methods, measures taken by three qualified observers were analysed using an intra-class correlation coefficient (ICC) method. The 3D registration method showed excellent reliability (ICC > 0.75) in glenoid implant inclination (0.97), version (0.98) and screw volume in bone (0.99). Conventional methods showed poor reliability (ICC < 0.4); CT-slice inclination (0.02), version (0.07), percentage of screw in bone (0.02) and for radiographic inclination (0.05) and percentage screw in bone (0.05). This CT registration of post-operative to pre-operative novel method for quantitatively assessing reverse shoulder arthroplasty glenoid implant positioning and screw percentage in bone, showed excellent inter-observer reliability compared to conventional 2D approaches. It overcomes metal-artifact limitations of post-operative CT evaluation.
antibiotics were withheld until cultures obtained, at least four fluid and tissue cultures were submitted, frozen sections were obtained of any tissue grossly suspicious for infection, and the surgeons’ pre-, intra-, and post-operative suspicion for infection were recorded. Samples were observed for growth for 28 days. All cases were reviewed at a mean follow-up of 4.2 months (range, 1–12). Comparisons were made between infection cases and “clinically Insignificant” cases, with respect to: (1) risk factors, (3) symptoms/signs of infection, (2) active range-of-motion, (2) Simple Shoulder Test (SST) scores, values of (3) WBC, (4) ESR and (5) CRP, number of positive cultures for (6) P acnes and (7) other organisms and (8) subjective pre-operative, intra-operative and postoperative suspicion for occult infection.
The purpose of this study was two-fold: 1) to examine perioperative prospective changes in pain, disability and psychosocial variables in ACL reconstructed recreational athletes over the pre-op to eight week post-op period. 2) to see what variables will predict greatest disability at eight weeks post-op. All participants were recreational athletes at the time of their injuries who had patella-autograft procedure at the the Queen Elizabeth II Health Sciences Centre. Fifty-four patients (twenty-nine males; mean age = 25.4 years, SD = 8.08). Mean education was fourteen years (SD = 2.08), 32%(17) were married, 67%(36) single, and 1% was divorced. 94%(51) of the sample was Caucasian, 3%(2) Black, and 1% Asian. One quarter reported their ACL injury was due to sport-based contact, with non-contact sporting activity reported at 76%(41). All participants completed measures of pain, depression, pain catastrophizing, state anxiety pre-op, on days one and two following surgery and again at eight weeks post-op. Disability was assessed pre-op and eight weeks post-op. Pain was varied across comparisons with preoperative pain increased twenty-four and forty-eight-hour post-op. Pain at forty-eight-hours postoperative was significantly higher than pain reported at eight-weeks post-op. Catastrophizing did not differ from the pre-op to twenty-four-hour post-op but did drop from twenty-four to forty-eight-hours and forty-eight-hours to eight-weeks post-op. Pre-op depression increased twenty-four-hour post-op, but not from twenty-four to forty-eight-hours and declined at eight-weeks. Anxiety increase pre-op to twenty-four-hours but not from twenty-four to forty-eight-hours but did drop from forty-eight-hours to eight-weeks.Disability did not change over time. Regression showed age or gender did not predict disability but forty-eight hour pain and catastrophizing did. These data indicate that pain and psychological variables change over time of ACL recovery. Results suggest that pain and distress peek during acute post-op period. As well, post-op catastrophizing predicts disability at eight weeks post-op which may indicate that catastrophizing may be related to behaviours related to slower recovery following ACL reconstructive surgery.
The purpose of this study was to review the results of biceps tenodesis and biceps reinsertion in the treatment of type II SLAP lesions. We conducted a retrospective cohort study of a continuous series of patients. Only isolated type II SLAP lesions were included: twenty-five cases from January 2000 to April 2004. Exclusion criteria included associated instability, rotator cuff rupture and previous shoulder surgery. Ten patients (ten men) with an average age of thirty-seven years (range, 19–57) had a reinsertion of the long head of the biceps tendon (LHB) to the labrum with two suture anchors. Fifteen patients (nine men and six women) with an average age of fifty-two years (range, 28–64) underwent biceps tenodesis in the bicipital groove. All patients were reviewed by an independent examiner. In the reattachment group, the average follow-up was thirty-five months (range, 24–69); three patients underwent subsequent biceps tenodesis for persistent pain, three others were disappointed because of an inability to return to their previous level of sport, and the remaining four were very satisfied. The average Constant score improved from sixty-five to eighty-three points. In the tenodesis group, the average follow-up was thirty-four months (range, 24–68). No patient required revision surgery. Subjectively, one patient was disappointed (atypical residual pain), two were satisfied and twelve were very satisfied. All patients returned to their previous level of sports, and the average Constant score improved from fifty-nine to eighty-nine points. The results of labral reattachment were disappointing in comparison to biceps tenodesis. Thus, arthroscopic biceps tenodesis can be considered as an effective alternative to reattachment in the treatment of isolated type II SLAP lesions. By moving the origin of the biceps to an extra-articular position, we eliminated the traction on the superior labrum and the source of pain; furthermore, range of motion and strength are unaltered allowing for a return to a pre-surgical level of activity.
The purpose was to evaluate the results of reverse shoulder arthroplasty (RSA) in proximal humerus fracture sequelae (FS). Multicenter retrospective series of forty-five consecutive patients operated between 1995 and 2003. Types of FS included: cephalic collapse and necrosis (n=8), chronic locked dislocation (n=5), surgical neck nonunion (n=7), severe malunion (twenty), and isolated greater tuberosity malunion (n=3). Twenty-six patients had surgical treatment of the initial fracture and seventeen had non-surgical treatment; thirty-three Delta and ten Aequalis reverse prosthesis were implanted. Mean age at surgery was seventy-three years (range, fifty-seven to eighty-six). Forty-three patients were available for clinical and radiologic evaluation with a mean follow-up of thirty-nine months (range, twenty-four to ninety-five). Nine re-operations (21%) and ten complications (23%) were encountered, including four infections (leading to two resection-arthroplasties), two instabilities, one glenoid fracture (converted to hemiarthroplasty) and one axillary nerve palsy. Thirty-six patients (83%) were satisfied or very satisfied with their result. The adjusted Constant score improved from 29% preoperatively to 75% postoperatively (p<
0.0001), the Constant score for pain from fou to twelve points (p<
0.0001), and active anterior elevation from 59° to 114° (p<
0.0001). Active rotations were limited. A positive postoperative hornblower test negatively influenced Constant score (forty-two points compared to 61.5 points, p=0.004) and external rotation (−6° compared to 15°, p=0.004). The lowest functional results were observed in surgical neck nonunions (with five complications) and isolated greater tuberosity malunions. In type four fracture sequelae, patients who had an osteotomy or resection of the GT (n=9) had better forward flexion (140° compared to 110°, p=0.026) and better Constant score (sixty-three points compared to forty-six points, p=0.07). RSA can be a surgical option in elderly patients with FS, specifically for those with severe malunion (type four fracture sequelae) where hemiarthroplasty gives poor results. By contrast, surgical neck nonunions (type three) and isolated greater tuberosity malunions are at risk for low functional results. The surgical technique and the remaining cuff muscles (teres minor) are important prognostic factors. Functional results are lower and complications/reoperations rates are higher than those reported for RSA in cuff tear arthritis.
The purpose of this study is to report the results of arthroscopic Bankart repair following failed open treatment of anterior instability. We performed a retrospective review of twenty-two patients with recurrent anterior shoulder instability (i.e. subluxations or dislocations, with or without pain) after open surgical stabilization. There were seventeen men and five women with an average age of thirty-one years (range, 15–65). The most recent interventions consisted of sixteen osseous transfers (twelve Latarjet and four Eden-Hybinette), three open Bankart repairs and three capsular shifts. The causes of failure were additional trauma in twelve patients and complications related to the bone-block in thirteen (poor position, fracture, pseudarthrosis or lysis). All patients were noted to have distension of the anterior-inferior capsular structures. Labral re-attachment and capsulo-ligamentous re-tensioning with suture anchors was performed in all cases with an additional rotator interval closure in four patients and an inferior capsular plication in twelve patients; the bone block screws were removed in eight patients. At an average follow-up of forty-three months (range, twenty-four to seventy-two months), nineteen patients were evaluated by two independent observers. One patient had recurrent subluxation, and two patients had persistent apprehension. Anterior elevation was unchanged, and loss of external rotation (RE1) was 6°. Nine patients returned to sport at the same level; all patients returned to their previous occupations, including the six cases of work-related injury. Eighty-nine percent were satisfied or very satisfied; the subjective shoulder value (SSV) was 83% ± 23%; the Walch-Duplay, Rowe and UCLA scores were 85 ± 21, 81 ± 23 and 30 ± 7 points respectively. The number of previous interventions did not influence the results. Eight patients (42%) were still painful (six with light pain and two with moderate pain). Arthroscopic revision of open anterior shoulder stabilization gives satisfactory results. The shoulders are both stable and functional. While the stability obtained with this approach is encouraging, our enthusiasm is tempered by some cases of persistent pain.
The complications of prostheses for fractures of the proximal humerus are understudied because the experience of each shoulder surgeon is limited and a standardised registration protocol is not yet available. A prospective study on complications in shoulder arthroplasty for fracture is, therefore, essential to explore variables that influence outcome. The purpose of this study is to report our experience with complications following arthroplasty for proximal humeral fractures. In a multicenter study, four hundred and six patients treated with arthroplasty for proximal humeral fracture were prospectively followed during a nine year period; three hundred patients with a minimum of two years follow-up, at an average of forty-five months (range, 24–117), were available for review. Objective results were graded with the Constant score and range of motion. Subjective results were reported according to patient satisfaction. At follow-up, the average Constant score was fifty-four points (range, 14–95) and active forward elevation was 103° (range, 10°–180°). Eighty-one percent of patients were satisfied or very satisfied. We observed a 59% rate of late (after three months) complications, including a high rate of tuberosity-related complications (72% malunion or nonunion). Initial tuberosity malposition was present in 35% of the patients. Secondary migration despite initial good positioning was observed in 24%. Tuberosity complications were associated with poor final Constant score, poor range of motion and shoulder pain (p=0.001 for all items). A re-operation was performed in 5.3% of the cases. Patients who were mobilised according to the ‘early passive motion’ concept had double the incidence of secondary tuberosity migration, compared to those that were initially immobilised (14% versus 27%, p=0.004). Tuberosity complications are the most frequent late complication and they are associated with poor functional results. It is, therefore, incumbent upon the surgeon to maximise healing with adequate fixation of the tuberosities, followed by sufficient immobilization.
The objective of this study is to report the epidemiology and results of treatment of deep infection after a reverse shoulder arthroplasty. This is a multicenter retrospective study involving 457 reverse prostheses performed between 1992 and 2002. Fifteen patients (3%) (mean age 71 ± 9 years) presented with a deep infection. Eight were primary arthroplasties and seven were revision procedures. There were five associated peri-operative fractures and three early postoperative complications requiring surgical treatment. Infection was treated by debridement (n=4), prosthetic resection (n=10) or two-stage revision (n=1). The infection rate was 2% (8/363) for a primary reverse arthroplasty and 7% (7/94) for revisions. The infection was diagnosed at a mean of seventeen months (range, one to fifty-seven) post-operatively, corresponding to two acute, five sub-acute and eight chronic infections. The most common pathogen was P. acnes in six cases (40%). At a mean follow-up of thirty-four ± nineteen months, there were twelve remissions (80%) and three recurrent infections. The two acute infections (one debridement and one resection) and the eight chronic infections (seven resections and one two-stage revision) were in remission. Among the five sub-acute infections, the two resections were in remission, whereas the three debridements recurred. Overall, the ten resections were in remission with seven patients disappointed and three satisfied, a mean Constant score of thirty-one ± eight points and a mean active anterior elevation of 53 ± 15°. The two-stage exchange was in remission but remained disappointed with a Constant score of twenty-seven points and an active anterior elevation of 90°. Infection compromises the functional results of the reverse prosthesis whatever the treatment performed. Acute infections appear to be satisfactorily treated by debridement or resection. Both resection and two-stage revision can successfully treat sub-acute and chronic infection; however, debridement alone is ineffective and not recommended. There is a high rate of infection when the reverse prosthesis is used in revision arthroplasty. Prevention, by looking for such infection before surgery and by performing a two-stage procedure is recommended in the case of any uncertainty.
The purpose of this study is to catalogue humeral problems with reverse total shoulder arthroplasty and define their influence on outcome. A multicenter retrospective review of 399 reverse humeral arthroplasties implanted between January 1994 and April 2003, yielded seventy-nine patients with humeral problems. We define a clinical humeral problem as an event that alters the expected rehab or postoperative course. Perioperative problems are fractures within the stem zone while postoperative problems involve fractures distal to the stem, prosthetic disassembly and subsidence. Radiologic problems include humeral loosening and radiolucencies of greater than 2 mm that have not had a clinical impact. All radiographs were available and reviewed by three orthopaedic surgeons. Objective results were rated according to the Constant score; active forward flexion and external rotation were recorded; and subjective outcome was noted. We identified twenty-six intra-operative fractures and eleven postoperative fractures. There were four cases of disassembly, three cases of subsidence, and fifteen cases of radiographic loosening. At a mean follow-up of forty-seven months, average active elevation was 111.3 degrees, external rotation was 7.0 degrees, and absolute Constant score improved from 21.9 to 50.1 points. Seventy-one percent of the patients were satisfied or very satisfied. Intra-operative humeral fractures were associated with poor final Constant score (42.3), poor range of motion and increased shoulder pain (p=0.001 for all items). Constant score for those revision patients who experienced a fracture was lower by 9.6 points (p=0.0347) than those patients who underwent a reverse prosthesis for revision surgery without a fracture. Constant score for those patients with a postoperative fracture averaged 47.2 (range, 8–70). A re-operation was performed in seven of the cases (9%). Intra-operative humeral fractures occur commonly when a reverse prosthesis is indicated for revision; humerotomy is not protective, however, and is not recommended for all humeral revisions. Fractures, either intraoperative or post-operative, result in lower Constant scores. Any patient who received an intervention for a humeral problem yielded a lower constant score. While postoperative Constant scores improved in all categories, they were lower than those patients who did not sustain a humeral complication.
The purpose of this study was to evaluate outcome following arthroscopic biceps tenotomy or tenodesis for massive irreparable rotator cuff tears associated with biceps lesions. This is a retrospective study of sixty-eight consecutive patients (mean age 68 ± 6 years) with seventy-two irreparable rotator cuff tears treated with arthroscopic biceps tenotomy (thirty-nine cases) or tenodesis (thirty-three cases). All patients were evaluated clinically and radiographically at a mean follow-up of thirty-five months (range, 24–52). Fifty-three patients (78%) were satisfied. Constant score improved from forty-six to sixty-seven points (p<
0.001). Presence of a healthy, intact teres minor on preoperative imaging correlated with increased postoperative external rotation (40 vs. 18°, p<
0.05) and higher Constant score (p<
0.05). Three patients with a pseudoparalyzed shoulder did not benefit from the procedure and did not regain active elevation above the horizontal level. By contrast, fifteen patients with painful loss of active elevation recovered active elevation. The acromiohumeral distance decreased 1 mm on average, and only one patient developed glenohumeral osteoarthritis. There was no difference between tenotomy and tenodesis (Constant Score sixty-one vs. seventy-three). A “Popeye” sign was clinically apparent in twenty-four tenotomy patients (61%), but none were bothered by it. Two patients required reoperation with a reverse prosthesis. Arthroscopic biceps tenotomy and tenodesis effectively treats severe pain or dysfunction caused by an irreparable rotator cuff tear associated with biceps pathology. Shoulder function is significantly lower if the teres minor is atrophic or fatty infiltrated. Pseudoparalysis or severe cuff arthropathy are contraindications.
We compared the initial strength of two techniques for repair of rotator cuff tears. Eight paired cadaveric shoulders with a standardized supraspinatus defect were studied. A transosseous suture and anchor repair was conducted on each side. Specimens were tested under cyclic loading, while fixation was monitored with an optical tracking technique. Mode of failure, number of cycles and load to failure were measured for 50% (5 mm) and 100% (10 mm) loss of repair. Anchors provide improved repair strength at 50% repair loss, in comparison to sutures (p<
0.05). Strength was unaffected by bone mineral density, age and gender. The purpose of this study was to compare the initial strength of two rotator cuff repair techniques. Repair strength with anchors was superior to sutures. Strength was unaffected by bone quality. Anchors, enabling a quicker, less invasive arthroscopic repair, offer improved fixation over sutures, which are more time consuming and invasive. Eight paired shoulders with a standardized supra-spinatus defect were randomized to anchor or suture repair, and subjected to cyclic loading. Repair migration was measured using a digital camera. Failure mode, cycles and load were measured for 50% and 100% loss of repair. Results were correlated with bone mineral density, age and gender. The anchors failed at the anchor-tendon interface, whereas the sutures failed through the sutures. Mean values for 50% loss of repair were 205.6 ± 87.5 cycles and 43.8 ± 14.8 N for the sutures, and 1192.5 ± 251.7 cycles and 156.3 ± 19.9 N for the anchors (p<
0.05). The corresponding values for 100% loss of repair were 2457.5 ± 378.6 cycles and 293.8 ± 27.4 N for the sutures, and 2291.9 ± 332.9 cycles and 262.5 ± 28.0 N for the anchors (p>
0.05). These results did not correlate with bone quality. This study has demonstrated that anchors provide improved repair strength, in comparison to sutures. This may be due to the relative less deformability of the anchors. Repair strength did not correlate with bone quality. This may be attributed to each repair failing primarily through the repair construct or at the anchor-tendon interface, and not through bone.